产品名称
肝素 钠, United States Pharmacopeia (USP) Reference Standard
grade
pharmaceutical primary standard
API family
enoxaparin
manufacturer/tradename
USP
application(s)
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
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Application
Enoxaparin Sodium Molecular Weight Calibrant B USP reference standard for use in specified quality tests and assays. Also used to plot calibration curves during the determination of molecular weight distribution and weight average molecular weight of Enoxapain Sodium using size exclusion chromatography (SEC).
General description
Enoxaparin Sodium is the sodium salt of a depolymerized heparin. It is obtained by alkaline depolymerization of heparin benzyl ester. Enoxaparin Sodium consists of a complex set of oligosaccharides that have not yet been completely characterized. The majority of the components have a 4-enopyranose uronate structure at the nonreducing end of their chain. Enoxaparin Sodium Molecular Weight Calibrant B reference standard is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including MSDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.
Other Notes
Sales restrictions may apply.
This product is part of the USP Biologics program.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
涉药品监管产品
此项目有
Enoxaparin Sodium
United States Pharmacopeia and National Formulary
United States Pharmacopeia, 48(3), 1623-1623 (2020)
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